Taiwan FDA registration 73dd790781667328318301036a3bf89e

"Leishi" positive pressure respiratory system

TW: “磊仕”陽壓呼吸系統
Taiwan flagTaiwan·Risk Class 2·RESPIRONICS INC.·Registered Mar 02, 2015 – Mar 02, 2030Active
Registration details
Analysis ID
73dd790781667328318301036a3bf89e
Customs Code
DHA05602703200
Company information
Manufacturer
RESPIRONICS INC.
Manufacturer Country
United States
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5905 Non-continuous respirators
Import Information
import
Dates and status
Registration Date
Mar 02, 2015
Expiry Date
Mar 02, 2030
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About this record

Access comprehensive regulatory information for "Leishi" positive pressure respiratory system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 73dd790781667328318301036a3bf89e and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including RESPIRONICS INC., RESPIRONICS INC.;; Respironics, Inc., and 5 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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